COLLAPSIN-INDUCED GROWTH CONE COLLAPSE MEDIATED BY AN INTRACELLULAR PROTEIN RELATED TO UNC-33

被引:625
作者
GOSHIMA, Y
NAKAMURA, F
STRITTMATTER, P
STRITTMATTER, SM
机构
[1] YALE UNIV,SCH MED,DEPT NEUROL,NEW HAVEN,CT 06520
[2] YALE UNIV,SCH MED,DEPT NEUROBIOL,NEW HAVEN,CT 06520
关键词
D O I
10.1038/376509a0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
COLLAPSIN(1), a member of the newly recognized semaphorin family(2-4), contributes to axonal pathfinding during neural development by inhibiting growth cone extension(1-5). The mechanism of collapsin action is poorly understood, Here we use a Xenopus laevis oocyte expression system to identify molecules involved in collapsin signalling, because several experiments have raised the possibility that heterotrimeric GTP-binding proteins might participate in these events(6-9). A collapsin response mediator protein of relative molecular mass (M(r)) 62K (CRMP-62) required for collapsin-induced inward currents in X. laevis oocytes is isolated. CRMP-62 shares homology with UNC-33, a nematode neuronal protein required for appropriately directed axonal extension(10-12), CRMP-62 is localized exclusively in the developing chick nervous system. Introduction of anti-CRMP-62 antibodies into dorsal root ganglion neurons blocks collapsin-induced growth cone collapse. CRMP-62 appears to be an intracellular component of a signalling cascade initiated by an unidentified transmembrane collapsin-binding protein.
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页码:509 / 514
页数:6
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